High Resolution Air Pollution Forecasting Using the NASA GEOS Model
Pollution forecasting aids in decision making for human health and agriculture studies.
Megan Damon↗
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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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San Diego Water Resources: Monitoring Pollution Plumes due to Storm and Wastewater Runoff in the San Diego Bay and Tijuana River Estuary to Inform Water Quality Management
Stormwater and wastewater runoff are a large source of pollutant discharge along the southern California coast and are a major concern to the health of local communities and ecosystems. In partnership with the Tijuana River National Estuarine Research Reserve and the California Department of Environmental Quality, NASA DEVELOP utilized satellite imagery to visualize and analyze the water quality of the Tijuana Estuary and southern California coast after major storm and wastewater events. Using Landsat 8 Operational Land Imager (OLI) and Sentinel-2 Multispectral Instrument (MSI), we estimated the extent and severity of plumes released from the Tijuana River Estuary. We used remotely sensed turbidity to map the extent of plumes, and used remotely sensed turbidity, Chlorophyll-a (chl-a), and colored dissolved organic matter (CDOM) to quantify and visualize stormwater, wastewater, and mixed plumes from 2013 to 2022. Furthermore, remotely sensed CDOM, turbidity, and chl-a were validated with in-situ data from NOAA and the San Diego Public Utilities in the San Diego coastal area to evaluate the accuracy of water quality data derived from satellite imagery. End products of this project include maps of stormwater, wastewater, and mixed plumes, tables illustrating the average area, CDOM, turbidity, and chl-a of each plume type, and validation graphs between satellite and in-situ data sources. These end products informed the environmental management of the Tijuana River National Estuarine Research Reserve and the public beaches in San Diego.
Ethan Gates↗
Tracking NO2 Pollution Changes Over Texas: Synthesis of In Situ and Satellite Observations
Nitrogen oxides (NO x ) are major air pollutants that play a crucial role in atmospheric chemistry. We compare Ozone Measuring Instrument's (OMI) NO 2 records with the in situ surface measurements from the Air Quality System of the US Environmental Protection Agency and the Texas Commission on Environmental Quality network in the state of Texas with the goal of understanding the correspondence of satellite and in situ surface observations and identifying the potential synergies between the two observing systems. Our analysis of over 40 in situ daily surface site observations, mostly from urban areas, and OMI daily observed data suggests a correlation ( r ) ranging between 0.2 and 0.8. The correlation improves considerably ( r > 0.5) for monthly average data. Weekly variation of surface NO 2 with a Sunday minimum is well captured by OMI tropospheric NO 2 column observations with similar weekend reductions. NO 2 trend in Texas during 2005–2019 is characterized by significant reductions of 20%–36% in highly populated cities and urban centers. However, a significant (up to 80%) increase was observed in oil and gas producing regions of the Permian and Eagle Ford Basins over the same period. In March–April of 2020, like the other US and global cities, Texas experienced up to 60% reduction in NO 2 levels in major cities due to travel restrictions imposed at local and national levels to contain the spread of COVID-19. Though such reduction is temporary, these reductions were significantly larger than those achieved in the past 16 years of OMI record suggesting that technological advancement can curtail NO x emissions.
Nitrogen dioxide (NO2)↗
Colorado Springs Health & Air Quality: Using Earth Observations to Monitor Wildfire Smoke and Air Pollution for Enhanced Air Quality Management in Colorado Springs, Colorado
An overview of our methods, findings, and takeaways for how we used Earth observations to monitor wildfire smoke and air pollution for enhanced air quality management.
Olivia Etherton↗
Upping the TEMPO on Air Pollution Observations from Space for Enhanced Science Applications
The Tropospheric Emissions: Monitoring of Pollution (TEMPO) mission was launched into Geostationary Earth Orbit (GEO) to 91°W longitude on April 7, 2023, and had a successful First Light period from July 31 – August 2 where the first hourly daytime scans across the TEMPO Field of Regard (FoR) covering greater North America were performed. First light images of nitrogen dioxide (NO2) were released to the public on August 24. In addition to NO2, TEMPO will provide hourly daytime observations of formaldehyde (HCHO), sulfur dioxide (SO2), ozone (O3), bromine (BrO), water vapor (H2O), and aerosols, at high spatial resolution (~2.0 x 4.75 km2) across the FoR. The hyperspectral ultraviolet-to-visible measurements from the TEMPO imaging grating spectrometer will permit an ozone profile retrieval capable of monitoring the diurnal evolution of ozone in the planetary boundary layer. The non-standard or special scan operations of TEMPO at sub-hourly frequency (e.g., 2-10 minutes) over selected slices of the FoR will further enhance monitoring capabilities during air quality disasters (e.g., wildfires, volcanic eruptions, dust storms, industrial accidents), research studies, and field campaign operations. A large diversity of stakeholders and end-users have been engaged in the TEMPO Early Adopters Program, supported by the NASA Applied Sciences Program, which aims to enhance health and air quality applications and maximize the societal benefit of TEMPO data when operational data becomes publicly available in the spring of 2024. Key outcomes from the Early Adopters Program include the pre-launch use of TEMPO proxy data to prepare the community for operational data, tailoring the data dissemination and visualization tools for the mission based on user needs, and enhancing the TEMPO special operations component of the mission through early adopter studies. This presentation will provide the latest TEMPO mission and Early Adopters Program updates, initiatives from the TEMPO special operations, and early demonstrations of science applications enabled through TEMPO data, while also showcasing the First Light imagery.
Air Quality↗
Mobile Observations of Ozone and Aerosols in Alabama: Southeastern US Summer Pollution and Coastal Variability
We present a detailed analysis of measurements of ozone (O 3 ) and aerosols collected using multiple platforms and instruments during a 5-day mini-campaign in Alabama, for improving our understanding of the chemistry and air quality in the Southeastern United States. Our study features the first on-road O 3 lidar profiling on highways and the coordinated airborne observations that captured O 3 and aerosol structures associated with synoptic weather conditions, stratospheric intrusions, wildfire smoke transport, and enhancements in urban areas. The Doppler wind lidar data suggest that the vertical structures and variability of O 3 and aerosols at Dauphin Island, a coastal site in the Gulf of Mexico, were related to both the synoptic flow and local-scale land-sea breeze circulation. The onshore gulf breeze, which typically started in the afternoon, helped to quickly dilute air pollutants near the surface, resulting in large gradients toward inland areas. In contrast, gradients were much smaller on days without a gulf breeze. O 3 and humidity were highly anti-correlated in the lower free troposphere, but weakly anti-correlated in the planetary boundary layer (PBL) suggesting more complicated emissions and sink of O 3 in the PBL. Our on-road and airborne measurement strategies to quantify the vertical and horizontal chemical gradients will be useful for future geostationary satellite validation.
Shi Kuang↗
Observation of Pollution Events at Low Altitude During TRACER-AQ – The Advantage of Adaptive Resolution Lidar
The TRACER-AQ campaign happened in August-September 2021 in Houston, Texas. Its objective was to better understand the pollution events in the coastal environment and to evaluate models and satellite observations. As a supporting instrument, NASA’s Langley Mobile Ozone Lidar (LMOL) was installed on the Houston campus, adjacent to University of Houston’s air-quality site, and performed observations of ozone and aerosols. Co-located instrumentation included a Pandora spectrophotometer, in-situ trace-gas measurements, and ozonesonde launches. Thanks to an adaptive resolution retrieval scheme, LMOL was able to detect thin-layer O3 structures at low (~200m) altitude that are not captured by the ozonesondes, and would ordinarily be missed with traditional coarse TOLNet lidar vertical averaging. We show that some of these features are not present in the models and are likely coming from local, industry-generated, emissions.
Guillaume Gronoff↗
Synergy of Urban Heat, Pollution, and Social 1 Vulnerability in One of America’s Most Rapidly 2 Growing Cities: Houston, We Have a Problem
During the first two decades of the twenty-first century, we analyze the expansion of 23urban land cover, urban heat island (UHI), and urban pollution island (UPI) in the Houston 24Metropolitan Area (HMA) using land cover classifications derived from Landsat and land/aerosol 25products from NASA's Moderate Resolution Imaging Spectroradiometer. Our approach involves 26both direct utilization and fusion with in situobservations for a comprehensive characterization.27We also examined how social vulnerability within the HMA changed during the study period and 28whether the synergy of UHI, UPI,and social vulnerability enhances environmental inequalities.
Andrew Blackford↗
Corrosion detector apparatus for universal assessment of pollution in data centers
A compact corrosion measurement apparatus and system includes an air fan, a corrosion sensor, a temperature sensor, a humidity sensor, a heater element, and an air flow sensor all under control to monitor and maintain constant air parameters in an environment and minimize environmental fluctuations around the corrosion sensor to overcome the variation commonly encountered in corrosion rate measurement. The corrosion measurement apparatus includes a structure providing an enclosure within which are located the sensors. Constant air flow and temperature is maintained within the enclosure where the corrosion sensor is located by integrating a variable speed air fan and a heater with the corresponding feedback loop control. Temperature and air flow control loops ensure that corrosivity is measured under similar conditions in different facilities offering a general reference point that allow a one to one comparison between facilities with similar or different pollution levels.
47 OTHER INSTRUMENTATION↗
National Emission Standards for Hazardous Air Pollutants – Radionuclide Emissions Calendar Year 2020
The U.S. Department of Energy (DOE), National Nuclear Security Administration Nevada Field Office (NNSA/NFO) operates the Nevada National Security Site (NNSS) and the North Las Vegas Facility (NLVF). From 1951 through 1992, the NNSS was the continental testing location for U.S. nuclear weapons. Radionuclides in air from NNSS activities have been monitored since the initiation of atmospheric testing. After 1962, testing was limited to underground detonations, which greatly reduced radiation exposure to the public. Since the end of nuclear testing in 1992, radiation monitoring has focused on detecting airborne radionuclides from historically contaminated soils because this sources dominates the potential offsite dose. These radionuclides are derived from re-suspension of soil (primarily by wind) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of legacy-related tritium are also emitted to air at the NLVF, an NNSS support complex in North Las Vegas. To protect the public from harmful levels of manmade radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP), specifically the National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities (40 CFR 61, Subpart H, 2020) limits the release of radioactivity from a DOE facility to that which would cause 10 millirem per year (mrem/y) effective dose equivalent (EDE) to any member of the public. This limit does not include radiation unrelated to NNSS activities. Unrelated doses could come from naturally occurring radioactive elements, from sources such as medically or commercially used radionuclides, or from sources outside of the United States, such as Japan’s Fukushima nuclear power plant, which was damaged in 2011. NNSA/NFO demonstrates compliance with the NESHAP limit by reporting environmental measurements of radionuclide air concentrations at critical receptor locations on the NNSS. This alternative was proposed and formerly submitted to the U.S. Environmental Protection Agency (EPA) in 2001 (EPA 2001a) and has been the method used to demonstrate compliance with the 40 CFR 61.92 dose standard since 2005. Six locations on the NNSS have been established to act as critical receptor locations to demonstrate compliance with the NESHAP limit. These locations are closer to radionuclide releases than where the public resides so they act as protective substitutes for public receptor locations. Compliance is demonstrated if the measured annual average concentration is less than the NESHAP Concentration Level (CL) for Environmental Compliance listed in Table 2 of 40 CFR 61, Appendix E. For multiple radionuclides, compliance is demonstrated when the sum of the fractions (determined by dividing each radionuclide’s concentration by its CL and then adding the fractions together) is less than 1.0. The EPAapproved air transport model, called the Clean Air Package 1988 (CAP88-PC) is also used to calculate the effective dose equivalent to the maximally exposed individual from NNSS air emissions. CAP88-PC was also used to calculate the population dose, or the collective EDE (expressed as person-rem [roentgen equivalent man] per year [person-rem/y]) for all individuals combined who reside within 80 kilometers (km) of NNSS emission sources. In 2020, the potential dose from radiological emissions to air from both current and past NNSS activities was well below the 10 mrem/y dose limit. This is demonstrated by both the air sampling data collected at critical receptor air monitoring stations and CAP88-PC modeling. The average concentrations of radioactivity at air critical receptor stations ranged from 0.2% to a maximum of 4.2% of the allowed NESHAP limit. CAP88-PC modeling of all 2020 NNSS radionuclide emissions showed the maximally exposed individual to be in Amargosa Valley and this individual received a potential dose of 0.063 mrem/y. The collective dose was calculated to be 0.29 person-rem/year for the 521,300 people who lived within 80 km of NNSS emission sources.
99 GENERAL AND MISCELLANEOUS↗
Ambient air pollution: How much of estimated “prenatal exposure” is truly attributable to pre-birth exposures?
No abstract prepared.
54 ENVIRONMENTAL SCIENCES↗
3D graphene aerogels-supported Ag and Ag@Ag3PO4 heterostructure for the efficient adsorption-photocatalysis capture of different dye pollutants in water
Highlights: • 3D graphene aerogels-supported Ag and Ag@Ag3PO4 heterostructure are synthesized. • The composite is effective in adsorption-photocatalysis cationic and anionic dyes. • The apparent adsorption-photocatalysis removal sequence is NR > RhB > MB > MO. • The contributions of adsorption and photocatalysis is different for different dyes. • The composite exhibits the highest catalytic activities with excellent stability. - Abstract: In this paper, we successfully synthesized 3D graphene aerogels-supported Ag and Ag@Ag{sub 3}PO{sub 4} heterostructure (3D Ag/Ag@Ag{sub 3}PO{sub 4}/GA) by the hetero-growth of Ag{sub 3}PO{sub 4} on partly Ag nanoparticles in macroporous 3D graphene aerogels (3D GA), aiming for the efficient adsorption-photocatalysis capture of both cationic (RhB, MB, and NR) and anionic (MO) dyes from aqueous solutions. For the removal of different dyes, the contributions of adsorption and photocatalysis is different and the apparent removal sequence is NR > RhB > MB > MO on the prepared 3D Ag/Ag@Ag{sub 3}PO{sub 4}/GA. Compared with bare Ag{sub 3}PO{sub 4} particles, Ag{sub 3}PO{sub 4}/GO, and Ag/Ag@Ag{sub 3}PO{sub 4}/GO, the prepared 3D Ag/Ag@Ag{sub 3}PO{sub 4}/GA exhibits the highest catalytic activities for the visible light degradation of RhB and MO. The possible mechanism for improved photocatalytic degradation of dyes by the 3D Ag/Ag@Ag{sub 3}PO{sub 4}/GA is proposed based on the active species trapping experiments. Moreover, the good stability and convenient recycling of the prepared 3D Ag/Ag@Ag{sub 3}PO{sub 4}/GA composite further make it have potential application prospect in eliminating organic contaminants.
36 MATERIALS SCIENCE↗
Ecological risk assessment of elemental pollution in sediment from Tunku Abdul Rahman National Park, Sabah
Eleven (11) surface sediment samples were collected from Tunku Abdul Rahman National Park, Sabah. The neutron activation analysis (NAA) and inductively coupled plasma-mass spectrometry (ICP-MS) techniques were applied for the determinations metal contents and their distributions in sediment samples. The results shown that Arsenic (As) concentrations are enriched at all sampling stations except for station TAR 09, with enrichment factor (EF) values ranged from 1.1 to 7.2. The elements such as Cd, Cr, Sb and U showed enrichment at a few stations and other elements (Cr, Cu, Pb, Th, Zn) shown as background levels in all stations. Degrees of contamination in this study were calculated base on concentrations of six elements (As, Cd, Cr, Cu, Pb, and Zn). TAR 11 station can be categorized as very high degree of contamination with degree of contamination value of 43.2. TAR 07 station can be categorized as a considerable degree of contamination (contamination value of 16.9). Six stations (TAR 01, 03, 04, 05, 06, 08, 10) showed moderate degree of contamination, with contamination values ranging from 8.0 to 16.0. TAR 02 and TAR 09 stations showed low degree of contaminations (< 8.0). TAR 11 showed very high ecological risk index (R{sub I}) with RI value is 916. TAR 07 and TAR 10 showed moderate ecological risk index with R{sub I} value 263 and 213, respectively. Other stations showed low ecological risk with RI values ranging from 42.3 to 117 (< 150). Very high ecological risk index could give an adverse effect to the benthic organism. The data obtained from the enrichment factor, degree of contamination and ecological risk index provided vital information, which can be used for future comparison. Information from the present study will be useful to the relevant government agencies and authorities in preparing preventive action to control direct discharge of heavy metals from industries, agro-base activities and domestic waste to the rivers and the sea.
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTAN↗
Mercury-Pollution Induction of Intracellular Lipid Accumulation and Lysosomal Compartment Amplification in the Benthic Foraminifer Ammonia parkinsoniana
Not Available
59 BASIC BIOLOGICAL SCIENCES↗
Economic implications of incorporating emission controls to mitigate air pollutants emitted from a modeled hydrocarbon-fuel biorefinery in the United States
The implementation of the US Renewable Fuel Standard is expected to increase the construction and operation of new biofuel facilities. Allowing this industry to grow without adversely affecting air quality is an important sustainability goal sought by multiple stakeholders. However, little is known about how the emission controls potentially required to comply with air quality regulations might impact biorefinery cost and deployment strategies such as siting and sizing. In this study, we use a baseline design for a lignocellulosic hydrocarbon biofuel production process to assess how the integration of emission controls impacts the minimum fuel selling price (MFSP) of the biofuel produced. We evaluate the change in MFSP for two cases as compared to the baseline design by incorporating (i) emission controls that ensure compliance with applicable federal air regulations and (ii) advanced control options that could be used to achieve potential best available control technology (BACT) emission limits. Our results indicate that compliance with federal air regulations can be achieved with minimal impact on biofuel cost (~$0.02 per gasoline gallon equivalent (GGE) higher than the baseline price of $5.10 GGE -1 ). However, if air emissions must be further reduced to meet potential BACT emission limits, the cost could increase nontrivially. For example, the MFSP could increase to $5.50 GGE -1 by adopting advanced emission controls to meet potential boiler BACT limits. Finally, given tradeoffs among emission control costs, permitting requirements, and economies of scale, these results could help inform decisions about biorefinery siting and sizing and mitigate risks associated with air permitting.
29 ENERGY PLANNING, POLICY, AND ECONOMY↗
Pollution and Risk of PAHs in Surface Sediments from the Tributaries and Their Relation to Anthropogenic Activities, in the Main Urban Districts of Chongqing City, Southwest China
Concentrations, sources and risk of 16 priority polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments from 19 representative tributaries in a regional scale of Chongqing City. The total concentration of 16 PAHs (ΣPAHs) ranged from 221 to 3205 ng g{sup −1} with a mean of 1055 ng g{sup −1}. Most tributaries of the Jialing River exhibited significantly higher ΣPAHs concentrations (mean 1864 ng g{sup −1}) compared to those flowing into the Yangtze River (mean 787 ng g{sup −1}). Isomeric ratio and hierarchical clustering analysis showed combustion may impact sedimentary PAHs at most center sites of the City, while PAHs at most sites were mixed of petrogenic and pyrogenic sources. Toxicity equivalency concentration for carcinogenic PAH were 2–4 times more than the Dutch limit. More comprehensive assessment of safety is suggested to reduce environmental risk of PAHs in sediments.
54 ENVIRONMENTAL SCIENCES↗
Historical Pollution and Source Contributions of PAHs in Sediment Cores from the Middle Reach of Huai River, China
To investigate the spatial and historical distributions, and source contributions of polycyclic aromatic hydrocarbon (PAHs) from the middle reach of Huai River, 15 surface sediments and two sediment cores were analyzed. The Σ{sub 16} PAHs levels in surface sediments varied from 533.15 to 1422.83 ng/g dw, and from 413.27 to 43951.56 ng/g dw in individual sediment layer of sediment cores. The temporal trends of PAHs in sediment cores are the good indicators of the anthropogenic emissions over the last 60 years. The stable carbon isotope ratios of PAHs indicate the primary PAHs sources were the combustion of wood and coal during 1950s–1970s, and automobile exhausts and the coal combustion emissions in recent decades.
54 ENVIRONMENTAL SCIENCES↗
Reduction of greenhouse gas and criteria pollutant emissions by direct conversion of associated flare gas to synthetic fuels at oil wellheads
Not Available
29 ENERGY PLANNING, POLICY, AND ECONOMY↗